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Dmitry Pruss

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Chemicals & Drugs

Genes & Molecular Sequences

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Kajal Biswas; Karla R Bowles; Sandra S Burkett; R Andrew Byrd; Ranabir Das; Julie M Eggington; Neil Hunter; Betty K Martin; Susan L North; Dmitry Pruss; Huanyu Qiao; Benjamin B Roa; Scott C Sizemore; Eileen Southon; Stacey Stauffer; Lino Tessarollo; Richard J Wenstrup; Shyam K Sharan
Functional evaluation of BRCA2 variants mapping to the PALB2-binding and C-terminal DNA-binding domains using a mouse ES cell-based assay.
Douglas F Easton; Amie M Deffenbaugh; Dmitry Pruss; Cynthia Frye; Richard J Wenstrup; Kristina Allen-Brady; Sean V Tavtigian; Alvaro Monteiro; Edwin S Iversen; Fergus J. Couch; David E Goldgar
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.
Georgia Chenevix-Trench; Sue Healey; Sunil Lakhani; Paul Waring; Margaret Cummings; Ross Brinkworth; Amie M Deffenbaugh; Lynn Anne Burbidge; Dmitry Pruss; Thaddeus Judkins; Thomas Scholl; Anna Bekessy; Anna Marsh; Paul K Lovelock; Ming Wong; Andrea Tesoriero; Helene Renard; Melissa C Southey; John L Hopper; Koulis Yannoukakos; Melissa Brown; Douglas Easton; Sean V Tavtigian; David E Goldgar; Amanda B Spurdle
Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.

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All Publications

2012: Kajal Biswas; Karla R Bowles; Sandra S Burkett; R Andrew Byrd; Ranabir Das; Julie M Eggington; Neil Hunter; Betty K Martin; Susan L North; Dmitry Pruss; Huanyu Qiao; Benjamin B Roa; Scott C Sizemore; Eileen Southon; Stacey Stauffer; Lino Tessarollo; Richard J Wenstrup; Shyam K Sharan
Functional evaluation of BRCA2 variants mapping to the PALB2-binding and C-terminal DNA-binding domains using a mouse ES cell-based assay.
Human molecular genetics 2012;21(18):3993-4006.
2007: Douglas F Easton; Amie M Deffenbaugh; Dmitry Pruss; Cynthia Frye; Richard J Wenstrup; Kristina Allen-Brady; Sean V Tavtigian; Alvaro Monteiro; Edwin S Iversen; Fergus J. Couch; David E Goldgar
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.
American journal of human genetics 2007;81(5):873-83.
2006: Georgia Chenevix-Trench; Sue Healey; Sunil Lakhani; Paul Waring; Margaret Cummings; Ross Brinkworth; Amie M Deffenbaugh; Lynn Anne Burbidge; Dmitry Pruss; Thaddeus Judkins; Thomas Scholl; Anna Bekessy; Anna Marsh; Paul K Lovelock; Ming Wong; Andrea Tesoriero; Helene Renard; Melissa C Southey; John L Hopper; Koulis Yannoukakos; Melissa Brown; Douglas Easton; Sean V Tavtigian; David E Goldgar; Amanda B Spurdle
Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.
Cancer research 2006;66(4):2019-27.
2005: Thaddeus Judkins; Brant C Hendrickson; Amie M Deffenbaugh; Kristilyn Eliason; Benoît Leclair; Michael J Norton; Brian E Ward; Dmitry Pruss; Thomas Scholl
Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations.
Cancer research 2005;65(21):10096-103.
2003: Brant C Hendrickson; Dmitry Pruss; E Lyon; Thomas Scholl
Application of haplotype pair analysis for the identification of hemizygous loci.
Journal of medical genetics 2003;40(5):346-7.
2002: Thomas S Frank; Amie M Deffenbaugh; Julia E Reid; Mark Hulick; Brian E Ward; Beth Lingenfelter; Kathi L Gumpper; Thomas Scholl; Sean V Tavtigian; Dmitry Pruss; Gregory C Critchfield
Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2002;20(6):1480-90.
2000: Michael T Pyne; Arthur R Brothman; Brian Ward; Dmitry Pruss; Brant C Hendrickson; Thomas Scholl
The BRCA2 genetic variant IVS7 + 2T-->G is a mutation.
Journal of human genetics 2000;45(6):351-7.
1999: Michael T Pyne; Dmitry Pruss; Brian E Ward; Thomas Scholl
A characterization of genetic variants in BRCA1 intron 8 identifies a mutation and a polymorphism.
Mutation research 1999;406(2-4):101-7.
1999: Thomas Scholl; Michael T Pyne; Brian Ward; Dmitry Pruss
Biochemical and genetic characterisation shows that the BRCA1 IVS20 insertion is a polymorphism.
Journal of medical genetics 1999;36(7):571-2.
1997: D Shattuck-Eidens; Arnold Oliphant; M McClure; celeste mcbride; J Gupte; Todd Rubano; Dmitry Pruss; Sean V Tavtigian; David Teng; N Adey; M Staebell; Kathi L Gumpper; R Lundstrom; Mark Hulick; M Kelly; J Holmen; B Lingenfelter; S Manley; F Fujimura; M Luce; Brian Ward; Lisa A Cannon-Albright; L Steele; Kenneth Offit; A Thomas
BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.
JAMA : the journal of the American Medical Association 1997;278(15):1242-50.